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| Name | Class |
|---|---|
| Photocure | INDUSTRY |
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The goal of this clinical trial is to learn if photodynamic diagnosis (PDD) performed using violet light after intra-vesical instillation of hexaminolaevulinic acid (Hexvix 85mg/50ml) is more sensitive than the standard white light tecnique in detection of malignant bladder tumour.
Patients will be randomised to:
Non-muscle invasive pT1 high-grade (HG) bladder cancer (NIMBC) represents a challenge for the urologists due to its aggressive behavior, with a marked tendency to recur after transurethral resection of the bladder (TURB) and even progress to muscle-invasive disease. To limit the risk of upstaging and to provide more clinical information indispensable for the decision-making process, international guidelines strongly recommend a re-TURB to be performed within 2-6 weeks from the first resection in all pT1HG tumors. However, not all the published literature agrees on the value of re-TURB wich is also an invasive and morbid procedure, requires a general or locoregional anesthesia and, like all surgical procedure, it is not free of risks and complications. There is, therefore, an unmet need for improving the quality and completeness of TURB which may have an impact on the necessity of Re-TURB. It has been confirmed that fluorescence-guided biopsy and resection (photodynamic diagnosis-PDD) are more sensitive than conventional procedures for the detection of malignant tumours, particularly for CIS. PDD is performed using violet light after intra-vesical instillation of hexaminolaevulinic acid (Hexvix 85mg/50ml).To date, no randomized controlled trials (RCTs) have been conducted aiming to compare the completeness of TURB with PDD compared to TURB with standard white light (WL).
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Photodynamic diagnosis using Hexvix | Experimental | Transurethral resection of the bladder (TURB) is performed using photodynamic diagnosis (PDD) which involves the of use the study drug (Hexvix) to allow for better visualisation and subsequent resection |
|
| White light | No Intervention | Transurethral resection of the bladder (TURB) is performed using the standard white light procedure |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Transurethral resection of the bladder performed with PDD tecnique and Hexvix | Procedure | For the execution of PDD cystoscopy in blue light, it is necessary to use the study drug (Hexvix) which, after intravesical instillation, causes an accumulation of porphyrins in the lesions of the bladder wall at the intracellular level. The intracellular porphyrins are photoactive fluorescent compounds that emit red light when excited with blue light. Consequently, the preneoplastic and neoplastic lesions will emit a red luminescence against a blue background, allowing for better visualisation and subsequent resection. |
| Measure | Description | Time Frame |
|---|---|---|
| Residual disease and/or upstaging | Compare the completeness of TURB with PDD vs TURB with WL in terms of proportion of patients with residual disease and/or upstaging at re-TURB | 6 to 8 weeks from the intervention |
| Measure | Description | Time Frame |
|---|---|---|
| Number of Participants diagnosed with malignant lesions | Compare the detection of malignant lesions between PDD and WLC using high-definition (HD) equipment during both primary TURB and re-TURB | 6 to 8 weeks from the intervention |
| The European organization for reasearch and treatment of cancer quality of life questionnaire for patients with non-muscle invasive bladder cancern |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Francesco Soria | Contact | 0116336594 | francesco.soria@unito.it | |
| Lisa Giacometti | Contact | lisa.giacometti@cpo.it |
| Name | Affiliation | Role |
|---|---|---|
| Francesco Soria | AOU Città della Salute e della Scienza | Principal Investigator |
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All Individual Participant Data requests should be submitted to the corresponding author for consideration. Access to deidentified participant data may be granted following review, after the publication of major results
Data will be available after 6 months from major results publication and for the following 5 years
Data requests should be submitted to the corresponding author for consideration
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| ID | Term |
|---|---|
| D001749 | Urinary Bladder Neoplasms |
| ID | Term |
|---|---|
| D014571 | Urologic Neoplasms |
| D014565 | Urogenital Neoplasms |
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
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| ID | Term |
|---|---|
| C419924 | 5-aminolevulinic acid hexyl ester |
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Randomised controlled trial. Randomization will be stratified based on the dedicated surgeon performing the procedure. Allocation will be at a 1:1 ratio between the two arms
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The scale range from 24 (better outcome) to 96 (worse outcome) |
| from date of randomization until 20 weeks from randomization |
| EQ-5D-5L | The scale range from 5 (better outcome) to 25 (worse outcome) | from date of randomization until 20 weeks from randomization |
| EQ VAS | A self-rating question of overall health status, measured on a 0 (worse outcome) to 100 (better outcome) visual analogue scale | from date of randomization until 20 weeks from randomization |
| Adverse events | Assess treatment changes and adverse events associated with each technique | from date of randomization until 20 weeks from randomization |
| D052776 |
| Female Urogenital Diseases |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
| D001745 | Urinary Bladder Diseases |
| D014570 | Urologic Diseases |
| D052801 | Male Urogenital Diseases |